Beyond genetics: epigenetic code in chronic kidney disease

被引:108
作者
Dwivedi, Rama S. [1 ]
Herman, James G. [2 ]
McCaffrey, Timothy A. [3 ]
Raj, Dominic S. C. [1 ]
机构
[1] George Washington Univ, Div Renal Dis & Hypertens, Washington, DC 20037 USA
[2] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[3] George Washington Univ, Div Genom Med, Dept Med, Washington, DC 20037 USA
关键词
chronic kidney disease; ESRD; genetics and development; mRNA; obesity; ABERRANT DNA METHYLATION; CPG-ISLANDS; CARDIOVASCULAR-DISEASE; RNA INTERFERENCE; FOLIC-ACID; HUMAN LUNG; GENOME; CANCER; EXPRESSION; PROMOTER;
D O I
10.1038/ki.2010.335
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Epigenetics refers to a heritable change in the pattern of gene expression that is mediated by a mechanism specifically not due to alterations in the primary nucleotide sequence. Well-known epigenetic mechanisms encompass DNA methylation, chromatin remodeling (histone modifications), and RNA interference. Functionally, epigenetics provides an extra layer of transcriptional control and plays a crucial role in normal physiological development, as well as in pathological conditions. Aberrant DNA methylation is implicated in immune dysfunction, inflammation, and insulin resistance. Epigenetic changes may be responsible for 'metabolic memory' and development of micro-and macrovascular complications of diabetes. MicroRNAs are critical in the maintenance of glomerular homeostasis and hence RNA interference may be important in the progression of renal disease. Recent studies have shown that epigenetic modifications orchestrate the epithelial-mesenchymal transition and eventually fibrosis of the renal tissue. Oxidative stress, inflammation, hyperhomocysteinemia, and uremic toxins could induce epimutations in chronic kidney disease. Epigenetic alterations are associated with inflammation and cardiovascular disease in patients with chronic kidney disease. Reversible nature of the epigenetic changes gives a unique opportunity to halt or even reverse the disease process through targeted therapeutic strategies. Kidney International (2011) 79, 23-32; doi: 10.1038/ki.2010.335; published online 29 September 2010
引用
收藏
页码:23 / 32
页数:10
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